Associated Papers
Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.
Tamana S et al.
Elife, 2022
36453528 (PubMed )
Supplement: elife-79713-supp2.xlsx › Input-Full_dataset
Distinctive mutation spectrum of the HBB gene in an urban eastern Indian population.
Sahoo SS et al.
Hemoglobin, 2014
Automated analysis of hemoglobin variants using nanoLC-MS and customized databases.
Das R et al.
Journal of Proteome Research, 2013
23692286 (PubMed )
Supplement: pr4000625_si_001.pdf
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